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Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II),  Cu(TMHD)2

Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II),  Cu(TMHD)2

  • Catalogue Number : SC10065
  • CAS Number : 14040-05-2
  • MDL Number : MFCD00058920
  • Molecular Formula : C22H38CuO4
  • Molecular Weight : 430.084
  • Purity : 98% Min.
  • Category : Catalysts and Ligands
Description

Catsyn offer gram to tons of Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II),  Cu(TMHD)2 | CAS 14040-05-2, its formula is C22H38CuO4, molecular weight is 430.084g/mol and the purity is usually 98% Min..

Synonyms : (2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATO)COPPER(II);2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONE COPPER(II) DERIVATIVE;BIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATO)COPPER(II);COPPER BIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATE);COPPER BIS(2,2,6,6-TETRAMETHYLHEPTANE-3,5-DIONE);COPPER BIS(DIPIVALOYMETHANATE);COPPER II 2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATE;COPPER(II) BIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATE);COPPER(II)-DPM;COPPER-THD;CU(TMHD)2;Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II),? Cu(TMHD)2

This substance (CAS No.: 14040-05-2) typically possesses a specific organic ligand or transition metal complex structure. Its molecular skeleton may contain aromatic rings, heteroatoms (such as nitrogen, oxygen, and phosphorus), or functional groups (such as amino, carboxyl, and phosphine groups). These structural units form a stable molecular configuration through covalent or coordinate bonds. Its physicochemical properties include specific melting points, boiling points, and solubility. It generally exhibits good solubility in organic solvents, while its solubility in polar solvents may be enhanced by hydrogen bonding or dipole interactions. Regarding electronic effects, electron-donating or electron-withdrawing groups in the molecule regulate the electron cloud density of the central metal through inductive or conjugation effects, thereby affecting its catalytic activity. In terms of energy level distribution, the interaction between ligand orbitals and metal d orbitals forms new molecular orbitals, lowering the activation energy of the reaction. The presence of conjugated systems (such as aromatic rings or conjugated double bonds) can enhance molecular stability and optimize the catalytic pathway through π-π stacking or electron delocalization effects. Its stability is influenced by steric hindrance, electronic effects, and coordination environment. Highly symmetrical structures or strong coordination bonds can significantly improve thermodynamic stability. Catalytic activity manifests in its accelerating effect on specific reactions (such as oxidation, reduction, and coupling), typically achieved by lowering transition state energy or stabilizing intermediates. Regarding coordination properties, this substance can act as a monodentate, bidentate, or multidentate ligand, forming stable complexes with metal centers through lone pairs of electrons or π orbitals. Coordination modes (such as chelation and bridging) directly affect catalytic selectivity. This substance has wide applications in materials science, organic synthesis, and OLEDs. As a catalyst, its core function is to accelerate chemical reaction processes. For example, in cross-coupling reactions, it promotes carbon-carbon bond formation through coordination-activation mechanisms, or in asymmetric catalysis, it induces highly enantioselective product formation through chiral environments, significantly improving synthesis efficiency and product purity. In OLED manufacturing, as a ligand, it can form luminescent complexes with rare earth or transition metals. By regulating the ligand structure, photoluminescence or electroluminescence performance can be optimized, achieving high color purity and high efficiency device performance. Its industry value lies in its role as a key intermediate or additive, which can reduce energy consumption in industrial production, decrease byproduct generation, and promote the development of green chemistry processes. In high-end manufacturing, its highly selective catalytic properties provide technical support for the precise synthesis of functional materials (such as pharmaceutical intermediates and polymer monomers). Furthermore, luminescent materials designed through coordination engineering can meet the stringent requirements of display technology regarding device lifespan, brightness, and color saturation, becoming a significant driving force for the upgrading of the optoelectronic industry.

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